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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_35bce0b8363dc3e87c11597734a15083
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-58
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-58
filingDate 2004-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a886b855f16031d041146bcdbbd9af68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_546c58a3bfc27947fb47cd9562ee6a16
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_569ca2465d40fc4cbe313b632cce0fb2
publicationDate 2007-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1791846-A1
titleOfInvention An improved process for the preparation of irinotecan hydrochloride trihydrate
abstract The invention relates to an improved process for the preparation of Irinotecan hydrochloride trihydrate of formula (4) of enhanced yield, purity by contacting 1-chlorocarbonyl-4-piperidinopiperidine hydrochloride with 7-ethyl-10 hydroxy-camptothecin [IRT-3 (synthetic)] to obtain crude Irinotecan which is subsequently purified by solvent treatment, obtaining purified irinotecan which is converted into irinotecan hydrochloride trihydrate and the invention also relates to a report of the compound 1-chlorocorbonyl-4-iperidinopiperidine hydrochloride of formula (1) and its process for preparation.
priorityDate 2004-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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